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CompletedNCT06732830

Clinical Trial to Assess the Effectiveness of I+Med's DayDrop Advanced Ophthalmic Drop

Clinical Trial for the Evaluation of I+Med's DayDrop Advanced Ophthalmic Drop in Improving Signs and Symptoms of Mild/Moderate Dry Eye

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
45 (actual)
Sponsor
i+Med S.Coop. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Clinical trial conducted with the aim of evaluating changes in the signs of dry eye through the change in the amount of tears produced, measured through the Schirmer test. It will be performed in 45 patients diagnosed with mild/moderate dry eye who meet the inclusion/exclusion criteria. Follow-up will be 12 weeks with a maximum of 4 visits.

Conditions

Interventions

TypeNameDescription
DEVICEDayDrop Advanced ophthalmic dropThe patient will administer 1 or 2 drops of DayDrop Advanced in each eye 3 times a day for 3 months.

Timeline

Start date
2022-12-21
Primary completion
2023-09-25
Completion
2023-09-25
First posted
2024-12-13
Last updated
2025-04-01

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT06732830. Inclusion in this directory is not an endorsement.

Clinical Trial to Assess the Effectiveness of I+Med's DayDrop Advanced Ophthalmic Drop (NCT06732830) · Clinical Trials Directory